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EXPERIMENTAL PROOF OF FORMATION OF IMINES AS INTERMEDIATES IN THE REDUCTION OF HYDRAZONES

机译:还原肼类中间体的矿物质形成的实验证明

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摘要

Imines derived from fluorenone do not undergo at pH 6-10 rapid hydrolysis. In this pH-range the imine is reduced in two one-electron steps. The fluorenone hydrazone and the corresponding N,N,N-trimethylhydrazonium ion is reduced in two steps: In the first three-electron step the two-electron cleavage of the N-N bond occurs. This wave is practically overlapped by the first one-electron wave of the imine. In the second one-electron wave the second reduction process of the imine takes place. This finding represents an experimental proof demonstrating that in hydrazones the N-N bond is cleaved first.
机译:衍生自芴酮的亚胺在pH 6-10时不会快速水解。在此pH范围内,亚胺在两个单电子步骤中被还原。分两个步骤还原芴酮和相应的N,N,N-三甲基hydr离子:在第一个三电子步骤中,发生N-N键的两电子裂解。该波实际上被亚胺的第一单电子波重叠。在第二单电子波中,发生亚胺的第二还原过程。这一发现代表了一个实验证据,表明在azo中,N-N键首先被裂解。

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